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rs61750168

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61750168(C;T)
Make rs61750168(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome17
Position8013918
GeneGUCY2D
is asnp
is mentioned by
dbSNPrs61750168
dbSNP (classic)rs61750168
ClinGenrs61750168
ebirs61750168
HLIrs61750168
Exacrs61750168
Gnomadrs61750168
Varsomers61750168
LitVarrs61750168
Maprs61750168
PheGenIrs61750168
Biobankrs61750168
1000 genomesrs61750168
hgdprs61750168
ensemblrs61750168
geneviewrs61750168
scholarrs61750168
googlers61750168
pharmgkbrs61750168
gwascentralrs61750168
openSNPrs61750168
23andMers61750168
SNPshotrs61750168
SNPdbers61750168
MSV3drs61750168
GWAS Ctlgrs61750168
Max Magnitude0
ClinVar
Risk rs61750168(G;G) rs61750168(T;T)
Alt rs61750168(G;G) rs61750168(T;T)
Reference Rs61750168(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GUCY2D
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.7917236C>T
CLNSRC UniProtKB (protein)
CLNACC RCV000084856.2,